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Biochemical and Biophysical Research Communications|October 8, 1999
Wild-type enzyme as a reporter of inhibitor binding by catalytically impaired mutant enzymesG S Basarab, D B Jordan
Bioorganic & Medicinal Chemistry Letters|January 15, 2000
Binding dynamics of two water molecules constrained within the scytalone dehydratase binding pocketD B Jordan, G S Basarab
Organic Letters|June 7, 2000
Solvolytic enolization of scytaloneG S Basarab, D B Jordan, Y J Zheng
Biochemistry|March 1, 2000
Stereochemistry of the enolization of scytalone by scytalone dehydrataseD B Jordan, Y J Zheng, B A Lockett, et al.
Bioorganic & Medicinal Chemistry Letters|April 1, 2000
Selection of a potent inhibitor of trihydroxynaphthalene reductase by sorting disease control dataD I Liao, G S Basarab, A A Gatenby, et al.
Structure (London, England : 1993)|May 9, 2001
Structures of trihydroxynaphthalene reductase-fungicide complexes: implications for structure-based design and catalysisD Liao, G S Basarab, A A Gatenby, et al.
Analytical Biochemistry|February 19, 1998
2,3-Dihydro-2,5-dihydroxy-4H-benzopyran-4-one: a nonphysiological substrate for fungal melanin biosynthetic enzymesJ E Thompson, G S Basarab, J Pierce, et al.
Bioorganic & Medicinal Chemistry Letters|July 1, 1999
Design of scytalone dehydratase inhibitors as rice blast fungicides: derivatives of norephedrineG S Basarab, D B Jordan, T C Gehret, et al.
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